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Overview
Description:
The Biotron Biometra Trio Heated Lid is a specialized accessory designed for use with compatible Biometra Trio Series thermal cycler systems. The heated lid is an integral component of the thermal cycler configuration, helping maintain appropriate temperature conditions within the sample chamber during thermal cycling workflows. Its design supports compatibility with the Biometra Trio Series, making it suitable for laboratory applications involving molecular biology research and sample processing.
Specifications:
Brand: Biotron
Product Name: Trio Heated Lid
Product Type: Heated Lid
Equipment Type: Thermal Cycler Accessory
Compatible Series: Biometra Trio Series
Function: Heated Lid Temperature Control
Application: Molecular Biology / Laboratory Research
Features:
Heated lid assembly configuration
Designed for Biometra Trio Series thermal cyclers
Supports thermal cycling workflows
Integrated thermal cycler accessory design
Suitable for compatible laboratory equipment
Intended for molecular biology research environments
Technical Details
| Brand | Biotron |
|---|---|
| Category | Heated Lid |
| Condition | Used |
| Cosmetic Condition | Good |
| OEM | Biotron |
| SKU | DA451-ITEM-K - P |
| Warranty | 30 - Warranty |
Need This Product Certified Patient-Ready?
If you require this product to be patient-ready certified, you can request a quote. Inspection, testing, repair, electrical safety testing, and calibration services are available through A Biomedical Service, Inc.
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Safety & Biomedical Inspection Notice
Shipping & Receiving Notice
Medical equipment may require inspection, functional verification, calibration, preventive maintenance, safety testing, or other evaluations following transportation and before being placed into service.
Upon receipt, the purchaser is responsible for inspecting the equipment for any shipping damage and determining whether any inspection, testing, calibration, preventive maintenance, or certification is necessary based on the manufacturer's recommendations, the receiving facility's policies, and all applicable laws and regulations.
The equipment should not be placed into clinical service or used for patient care until the purchaser has verified that it is safe, appropriate, and compliant for its intended use.
Biomedical Inspection Notice
Medical equipment should be evaluated by qualified personnel before being placed into clinical service. Depending on the type of equipment, the evaluation may include, as applicable:
- Electrical safety testing
- Functional performance verification
- Alarm verification (if applicable)
- Battery inspection or replacement (if applicable)
- Calibration verification (if applicable)
- Preventive maintenance
- Software configuration and system settings
- Verification of compatible accessories, consumables, and disposables
- Inspection for shipping or handling damage
- Compliance with the manufacturer's recommendations
- Compliance with the receiving facility's policies, procedures, and applicable regulatory requirements
Transportation, storage, handling, and installation may affect the performance of medical equipment. Reuse Medical recommends that the receiving facility inspect, test, and evaluate the equipment in accordance with the manufacturer's recommendations and the facility's biomedical engineering procedures before placing the equipment into clinical service or patient use.
